US4002425A - Water-insoluble monoazo dyestuffs - Google Patents

Water-insoluble monoazo dyestuffs Download PDF

Info

Publication number
US4002425A
US4002425A US05/597,018 US59701875A US4002425A US 4002425 A US4002425 A US 4002425A US 59701875 A US59701875 A US 59701875A US 4002425 A US4002425 A US 4002425A
Authority
US
United States
Prior art keywords
sub
weight
parts
carbon atoms
formula
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US05/597,018
Inventor
Ernst Heinrich
Horst Kindler
Joachim Ribka
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Cassella Farbwerke Mainkur AG
Original Assignee
Cassella Farbwerke Mainkur AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from DE19732352858 external-priority patent/DE2352858A1/en
Application filed by Cassella Farbwerke Mainkur AG filed Critical Cassella Farbwerke Mainkur AG
Priority to US05/597,018 priority Critical patent/US4002425A/en
Application granted granted Critical
Publication of US4002425A publication Critical patent/US4002425A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00—Monoazo dyes prepared by diazotising and coupling
    • C09B29/34—Monoazo dyes prepared by diazotising and coupling from other coupling components
    • C09B29/36—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds
    • C09B29/3604—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom
    • C09B29/3617—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom
    • C09B29/3621—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom from a pyridine ring
    • C09B29/3626—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom from a pyridine ring from a pyridine ring containing one or more hydroxyl groups (or = O)
    • C09B29/363—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom from a pyridine ring from a pyridine ring containing one or more hydroxyl groups (or = O) from diazotized amino carbocyclic rings

Definitions

  • the present invention relates to water-insoluble monoazo dyestuffs of the formula: ##STR2## wherein R is
  • the dyestuffs of this invention may be prepared by a process which comprises diazotising an amine of the formula: ##STR3## wherein R is as aforesaid, and coupling the diazotisation product with 3-cyano-4-methyl- 6-hydroxy-2-pyridone, i.e. the compound of the formula: ##STR4##
  • disperse dyestuffs When forming disperse dyestuffs, it can be of advantage to diazotise a mixture of two or more different amines of formula II and to couple the diazotisation product with 3-cyano-4-methyl-6-hydroxy-2-pyridone.
  • dyestuffs of formula I and the compounds of formula III it is possible for the dyestuffs of formula I and the compounds of formula III to exist in certain tautomeric forms and it is to be understood, that the present invention includes dyestuffs I and compounds III in all their respective possible tautomeric forms.
  • Compound III can be produced, as described by Bobbitt and Scola in J.Org.Chem. 25, 560, by the condensation of acetoacetic acid ethyl ester with cyanoacetamide in the presence of potassium hydroxide boiling methanol.
  • the amines of formula II which are employed as starting materials, can be produced, for example, by reacting p-nitrochlorobenzene of formula IV with an alcoholate of formula V to give a nitro product of formula VI and reducing this to an amine of formula VII. This is followed by acetylation of the amine to an acetylamine of formula VIII, which, after nitration to a compound of formula IX and saponification, gives the amine of formula II required as the starting product: ##STR5##
  • the dyestuffs according to the invention are particularly suitable for dyeing and printing shaped articles comprising numerous synthetic materials, for example, polyolefins, polyvinyl compounds, cellulose 21/2-acetate, cellulose triacetate, and, especially polyester materials, e.g. polyethylene glycol terephthalate.
  • synthetic materials for example, polyolefins, polyvinyl compounds, cellulose 21/2-acetate, cellulose triacetate, and, especially polyester materials, e.g. polyethylene glycol terephthalate.
  • polyester materials e.g. polyethylene glycol terephthalate
  • the dyeing of the said materials (more particularly in fibre form) with the dyestuffs according to the invention is suitably carried out from aqueous suspension in the presence of carriers at approximately 80° - 100° C, or in the absence of carriers at approximately 110° - 140° C, or by the "thermofixing" process at approximately 180° -230° C.
  • the printing of the said materials can be carried out by steaming the goods printed with the dyestuffs according to the invention in the presence of a carrier at approximately 80° - 110° C, or in the absence of a carrier at approximately 110° - 140° C, or by treating the goods by the "thermofixing" process at approximately 180° - 230° C.
  • the dyestuffs according to the invention are also suitable for dyeing the above-mentioned (hydrophobic) materials from organic solvents, and for bulk-dyeing.
  • the dyestuffs according to this invention possess greater tinctorial strength and/or better build-up capacity.
  • One hundred parts by weight of a polyester fabric based on polyethylene glycol terephthalate are introduced into the dyeing liquor thus obtained and the fabric is dyed for 11/2 hours at 130° C.
  • Example 1a Thirty parts by weight of the dyestuff obtained according to Example 1a, in a finely divided form, are incorporated into a printing paste which contains 45.0 parts by weight of carob bean flour, 6.0 parts by weight of sodium 3-nitrobenzene-sulphonate and 3.0 parts by weight of citric acid per 1,000 parts by weight.
  • a printing paste which contains 45.0 parts by weight of carob bean flour, 6.0 parts by weight of sodium 3-nitrobenzene-sulphonate and 3.0 parts by weight of citric acid per 1,000 parts by weight.
  • a polyethylene glycol terephthalate fabric is padded on a padder at 30° C with a liquor which contains 30 parts by weight of the dyestuff of the formula ##STR28## which had been brought to a finely divided state, 1.0 part by weight of polyacrylamide of K-value 120 and 0.5 part by weight of a polyglycol ether of oleyl alcohol and 968.5 parts by weight of water. After drying, fixing is carried out in a thermofixing frame for 60 seconds at 210° C. After subsequent rinsing and finishing as described in Example 1b, paragraph 3, an orange dyeing of very good fastness properties and very good build-up capacity is obtained.
  • Example 2b Following the procedure described in Example 1b, a polyethylene glycol terephthalate fabric is dyed with 1.0 part by weight of the finely disperse dyestuff of the formula ##STR32## obtained above, and is after-treated. A deep orange dyeing having very good tinctorial properties, especially very good fastness to light and to thermofixing and very good build-up capacity, is obtained. The dyestuff has very good pH-stability.
  • polyester material One hundred parts by weight of polyester material are treated for 30 minutes at 121° C in 1,500 parts by weight of tetrachloroethylene in which 2.0 parts by weight of the dyestuff described in Example 1a are dissolved.
  • the material is rinsed with warm and cold tetrachloroethylene and a strong orange dyeing of very good tinctorial properties is obtained.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Abstract

Dyestuffs of the formula: ##STR1## wherein R is A. ALKYL HAVING 3 TO 12 CARBON ATOMS;
B. alkenyl having 2 to 4 carbon atoms;
C. alkyl having 2 to 12 carbon atoms substituted by --O--(Cn H2n O)m --R1 wherein R1 is alkyl having 1 to 4 carbon atoms or alkenyl having 2 to 4 carbon atoms, n is 2, 3 or 4 and m is 0, 1 or 2;
D. alkenyl having 2 to 4 carbon atoms substituted by said --O--(Cn H2n O)m --R1 or
E. cycloalkyl having 5 or 6 carbon atoms or said cycloalkyl substituted by alkoxy having 1 to 4 carbon atoms; process of making said dyestuffs and process of dyeing hydrophobic synthetic materials therewith and resulting dyed materials.

Description

CROSS-REFERENCE TO RELATED APPLICATION
This application is a division of application Ser. No. 516,360 filed Oct. 21, 1974.
The present invention relates to water-insoluble monoazo dyestuffs of the formula: ##STR2## wherein R is
A. ALKYL HAVING 3 TO 12 CARBON ATOMS;
B. ALKENYL HAVING 2 TO 4 CARBON ATOMS;
C. ALKYL HAVING 2 TO 12 CARBON ATOMS SUBSTITUTED BY --O--(Cn H2n O)m--R1 wherein R1 is alkyl having 1 to 4 carbon atoms or alkenyl having 2 to 4 carbon atoms, n is 2, 3 or 4 and m is 0, 1 or 2;
D. ALKENYL HAVING 2 TO 4 CARBON ATOMS SUBSTITUTED BY SAID --O--(Cn H2n O)m--R 1 or
E. CYCLOALKYL HAVING 5 OR 6 CARBON ATOMS OR SAID CYCLOALKYL SUBSTITUTED BY ALKOXY HAVING 1 TO 4 CARBON ATOMS.
The dyestuffs of this invention may be prepared by a process which comprises diazotising an amine of the formula: ##STR3## wherein R is as aforesaid, and coupling the diazotisation product with 3-cyano-4-methyl- 6-hydroxy-2-pyridone, i.e. the compound of the formula: ##STR4##
When forming disperse dyestuffs, it can be of advantage to diazotise a mixture of two or more different amines of formula II and to couple the diazotisation product with 3-cyano-4-methyl-6-hydroxy-2-pyridone.
It is possible for the dyestuffs of formula I and the compounds of formula III to exist in certain tautomeric forms and it is to be understood, that the present invention includes dyestuffs I and compounds III in all their respective possible tautomeric forms.
Compound III can be produced, as described by Bobbitt and Scola in J.Org.Chem. 25, 560, by the condensation of acetoacetic acid ethyl ester with cyanoacetamide in the presence of potassium hydroxide boiling methanol.
The amines of formula II, which are employed as starting materials, can be produced, for example, by reacting p-nitrochlorobenzene of formula IV with an alcoholate of formula V to give a nitro product of formula VI and reducing this to an amine of formula VII. This is followed by acetylation of the amine to an acetylamine of formula VIII, which, after nitration to a compound of formula IX and saponification, gives the amine of formula II required as the starting product: ##STR5##
Examples of possible radicals R in formula V and hence also in formula II are:
--CH.sub.2 --CH.sub.2 --OCH.sub.3
--ch.sub.2 --ch.sub.2 --o--c.sub.4 h.sub.9(n)
--(CH.sub.2 --CH.sub.2 --O).sub.2 --CH.sub.3
--(ch.sub.2 --ch.sub.2 --o).sub.2 --c.sub.2 h.sub.5
--(ch.sub.2 --ch.sub.2 --o).sub.3--ch.sub.3
--(ch.sub.2 --ch.sub.2 -o).sub.3 --c.sub.3 h.sub.7(iso)
--CH.sub.2 --CH.sub.2 --CH.sub.3
__________________________________________________________________________
              ##STR6##                                                    
             ch.sub.2ch.sub.2ch.sub.2och.sub.3                            
              ##STR7##                                                    
             ch.sub.2chch.sub.2                                           
              ##STR8##                                                    
             ch.sub.2ch.sub.2ch.sub.2ch.sub.3                             
              ##STR9##                                                    
              ##STR10##                                                   
              ##STR11##                                                   
              ##STR12##                                                   
             ch.sub.2ch.sub.2ch.sub.2ch.sub.2och.sub.2ch.sub.3            
             ch.sub.2chchch.sub.3                                         
             (ch.sub.2).sub.4ch.sub.3                                     
              ##STR13##                                                   
             (ch.sub.2).sub.5ch.sub.3                                     
              ##STR14##                                                   
             (ch.sub.2).sub.6ch.sub.3                                     
              ##STR15##                                                   
             (ch.sub.2).sub.7ch.sub.3                                     
 ##STR16##        (ch.sub.2ch.sub.2ch.sub.2o).sub.2ch.sub.3               
                  (ch.sub.2ch.sub.2ch.sub.2o).sub.2c.sub.2 h.sub.5        
 ##STR17##        (ch.sub.2ch.sub.2ch.sub.2o).sub.3c.sub.2 h.sub.5        
(ch.sub.2).sub.9ch.sub.3                                                  
                  ch.sub.2chchoch.sub.3                                   
(ch.sub.2).sub.11ch.sub.3                                                 
                  ch.sub.2chchoch.sub.2ch.sub.2och.sub.3                  
 ##STR18##                                                                
                   ##STR19##                                              
 ##STR20##                                                                
                   ##STR21##                                              
 ##STR22##                                                                
                   ##STR23##                                              
 ##STR24##                                                                
__________________________________________________________________________
the dyestuffs according to the invention are particularly suitable for dyeing and printing shaped articles comprising numerous synthetic materials, for example, polyolefins, polyvinyl compounds, cellulose 21/2-acetate, cellulose triacetate, and, especially polyester materials, e.g. polyethylene glycol terephthalate. On these materials, they give, by the ordinary dyeing and printing processes, deep orange dyeings and prints with very good fastness properties, especially with very good fastness to light and to sublimation, and very good build-up capacity.
The dyeing of the said materials (more particularly in fibre form) with the dyestuffs according to the invention is suitably carried out from aqueous suspension in the presence of carriers at approximately 80° - 100° C, or in the absence of carriers at approximately 110° - 140° C, or by the "thermofixing" process at approximately 180° -230° C. The printing of the said materials can be carried out by steaming the goods printed with the dyestuffs according to the invention in the presence of a carrier at approximately 80° - 110° C, or in the absence of a carrier at approximately 110° - 140° C, or by treating the goods by the "thermofixing" process at approximately 180° - 230° C.
The dyestuffs according to the invention are also suitable for dyeing the above-mentioned (hydrophobic) materials from organic solvents, and for bulk-dyeing.
Compared to the dyestuffs described in German Published Specification (Offenlegungsschrift) No. 1,544,446, Example 4, which are obtained by coupling diazotised 3-nitro-4-amino-anisole or 3-nitro-4-amino-phenetole with 3-cyano-4-methyl-6-hydroxy-2-pyridone, the dyestuffs according to this invention possess greater tinctorial strength and/or better build-up capacity.
The following Examples illustrate the invention.
EXAMPLE 1
a. Twenty-one parts by weight of 3-nitro-4-amino-phenyl n-butyl ether of the formula ##STR25## are diazotised in 150 parts by weight of glacial acetic acid by means of 34.2 parts by weight of 41.3% strength nitrosylsulphuric acid at +15° C, with external cooling. The clear diazo solution is then allowed to run into a suspension of 16.5 parts by weight of 3-cyano-4-methyl-6-hydroxy-2-pyridone in 400 parts by weight of water and 120 parts by weight of sodium hydroxide solution of 33°Be strength. During the coupling, the reaction temperature is kept at 0° to +5° C by addition of approximately 500 parts by weight of ice. After completion of coupling, the resulting dyestuff is filtered off, rinsed with water and dried. It is a red powder which gives a red solution in concentrated sulphuric acid.
b. One part by weight of the finely disperse dyestuff of the formula ##STR26## thus obtained is stirred into 2,000 parts by weight of water. The pH value is adjusted to 5-6 with acetic acid and 4.0 parts by weight of ammonium sulphate and 2.0 parts by weight of a commercially available dispersing agent based on naphthalenesulphonic acid/formaldehyde condensate are added.
One hundred parts by weight of a polyester fabric based on polyethylene glycol terephthalate are introduced into the dyeing liquor thus obtained and the fabric is dyed for 11/2 hours at 130° C.
After subsequent rinsing, reductive after-treatment with an 0.2% strength alkaline sodium dithionite solution for 15 minutes at 70° - 80° C, rinsing and drying, a deep orange dyeing with very good tinctorial properties, especially very good fastness to light and to thermofixing, and very good build-up capacity, is obtained.
c. Thirty parts by weight of the dyestuff obtained according to Example 1a, in a finely divided form, are incorporated into a printing paste which contains 45.0 parts by weight of carob bean flour, 6.0 parts by weight of sodium 3-nitrobenzene-sulphonate and 3.0 parts by weight of citric acid per 1,000 parts by weight. Using this printing paste, an orange print of very good fastness properties is obtained on a triacetate fabric after printing, drying and fixing by pressure steaming for 15 minutes at 1.5 atmospheres gauge, rinsing and finishing, as described in paragraph 3 of Example 1b.
EXAMPLE 2
a. Following the procedure described in Examnple 1a, 25.6 parts by weight of 3-nitro-4-amino-phenyl [B-B'-methoxy)-ethoxy]-ethyl ether of the formula ##STR27## are diazotised and coupled with 16.5 parts by weight of 3-cyano-4-methyl-6-hydroxy-2-pyridone, and the product is isolated. The resulting dyestuff is a red powder which gives a red solution in concentrated sulphuric acid.
b. A polyethylene glycol terephthalate fabric is padded on a padder at 30° C with a liquor which contains 30 parts by weight of the dyestuff of the formula ##STR28## which had been brought to a finely divided state, 1.0 part by weight of polyacrylamide of K-value 120 and 0.5 part by weight of a polyglycol ether of oleyl alcohol and 968.5 parts by weight of water. After drying, fixing is carried out in a thermofixing frame for 60 seconds at 210° C. After subsequent rinsing and finishing as described in Example 1b, paragraph 3, an orange dyeing of very good fastness properties and very good build-up capacity is obtained.
EXAMPLE 3
a. Following the procedure described in Example 1a, 21.0 parts by weight of 3-nitro-4-amino-phenyl α-methyl-propyl ether of the formula ##STR29## are diazotised and coupled with 16.5 parts by weight of 3-cyano-4-methyl-6-hydroxy-2-pyridone, and the product is isolated. The resulting dyestuff is a red powder which gives a red solution in concentrated sulphuric acid.
b. Thirty parts by weight of the dyestuff obtained according to Example 3a, of the formula ##STR30## are incorporated, in a finely divided form, into a printing paste which contains 45.0 parts by weight of carob bean flour, 6.0 parts by weight of sodium 3-nitrobenzene-sulphonate and 3.0 parts by weight of citric acid per 1,000 parts by weight. Using this printing paste, a deep orange print of very good tinctorial properties, especially very good fastness to light and to thermofixing, and of very good build-up capacity, is obtained on a polyester fabric after printing, drying and fixing in a thermofixing frame for 45 seconds at 215° C, rinsing and finishing, as described in paragraph 3 of Example 1b.
EXAMPLE 4
a. Following the procedure described in Example 1a, 26.6 parts by weight of 3-nitro-4-amino-phenyl 2'-ethyl-n-hexyl ether of the formula ##STR31## are diazotised and coupled with 16.5 parts by weight of 3-cyano-4-methyl-6-hydroxy-2-pyridone, and the product is isolated. The resulting dyestuff is a red powder which gives a red solution in concentrated sulphuric acid.
b. Following the procedure described in Example 1b, a polyethylene glycol terephthalate fabric is dyed with 1.0 part by weight of the finely disperse dyestuff of the formula ##STR32## obtained above, and is after-treated. A deep orange dyeing having very good tinctorial properties, especially very good fastness to light and to thermofixing and very good build-up capacity, is obtained. The dyestuff has very good pH-stability.
EXAMPLE 5
One hundred parts by weight of polyester material are treated for 30 minutes at 121° C in 1,500 parts by weight of tetrachloroethylene in which 2.0 parts by weight of the dyestuff described in Example 1a are dissolved.
The material is rinsed with warm and cold tetrachloroethylene and a strong orange dyeing of very good tinctorial properties is obtained.
Orange dyeings of very good tinctorial properties are also obtained if, in the above example, the polyester material is replaced by 100 parts by weight of triacetate or 21/2-acetate material and this material is dyed for 45 minutes at 110° C or 45 minutes at 80° C, respectively.
The table which follows indicates further dyestuffs according to the invention, manufactured by coupling in accordance with the procedures of Examples 1 - 4, which give deep orange dyeings or prints, also having very good tinctorial properties, on polyester materials:
______________________________________                                    
 ##STR33##                                                                
No.    R                                                                  
______________________________________                                    
1      CH.sub.2CH.sub.2CH.sub.3                                           
        ##STR34##                                                         
3                                                                         
        ##STR35##                                                         
4                                                                         
        ##STR36##                                                         
5      (CH.sub.2).sub.4CH.sub.3                                           
6                                                                         
        ##STR37##                                                         
7      (CH.sub.2).sub.5CH.sub.3                                           
8                                                                         
        ##STR38##                                                         
9      (CH.sub.2).sub.6CH.sub.3                                           
10     (CH.sub.2).sub.7CH.sub.3                                           
11                                                                        
        ##STR39##                                                         
12     (CH.sub.2).sub.9CH.sub.3                                           
13     (CH.sub.2).sub.11CH.sub.3                                          
14     CHCH.sub.2                                                         
15     CH.sub.2CHCH.sub.2                                                 
16                                                                        
        ##STR40##                                                         
17     CH.sub.2CHCHCH.sub.3                                               
18     CH.sub.2CH.sub.2OCH.sub.3                                          
19     CH.sub.2CH.sub.2CH.sub.2OCH.sub.3                                  
20                                                                        
        ##STR41##                                                         
21                                                                        
        ##STR42##                                                         
22     CH.sub.2CH.sub.2OC.sub.3 H.sub.7(iso)                              
23     CH.sub.2CH.sub.2CH.sub.2OC.sub.4 H.sub.9(n)                        
24                                                                        
        ##STR43##                                                         
25     CH.sub.2CH.sub.2CH.sub.2CH.sub.2OC.sub.2 H.sub.5                   
26     CH.sub.2CH.sub.2CH.sub.2CH.sub.2OC.sub.4 H.sub.9(n)                
27     CH.sub.2CH.sub.2OCH.sub.2CHCH.sub.2                                
28     (CH.sub.2CH.sub.2O).sub.2CH.sub.3                                  
29     (CH.sub.2CH.sub.2O).sub.2C.sub.4 H.sub.9(n)                        
30     (CH.sub.2CH.sub. 2O).sub.3CH.sub.3                                 
31     (CH.sub.2CH.sub.2O).sub.3C.sub.2 H.sub.5                           
32     (CH.sub.2CH.sub.2CH.sub.2CH.sub.2O).sub.2CH.sub.3                  
33     (CH.sub.2CH.sub.2O).sub.2CH.sub.2CHCHCH.sub.3                      
34     (CH.sub.2CH.sub.2CH.sub.2O).sub.2CH.sub.3                          
35     (CH.sub.2CH.sub.2CH.sub.2O).sub.2C.sub.2 H.sub.5                   
36     (CH.sub.2CH.sub.2CH.sub.2O).sub.3C.sub.2 H.sub.5                   
37     CH.sub.2CHCHOCH.sub.3                                              
38     CH.sub.2CHCHOCH.sub.2CH.sub.2OCH.sub.3                             
39                                                                        
        ##STR44##                                                         
40                                                                        
        ##STR45##                                                         
41                                                                        
        ##STR46##                                                         
42                                                                        
        ##STR47##                                                         
43                                                                        
        ##STR48##                                                         
44                                                                        
        ##STR49##                                                         
______________________________________

Claims (3)

What is claimed is:
1. In the process of dyeing or printing a hydrophobic synthetic material, the improvement wherein the dyestuff is a water-insoluble monoazo dyestuff of the formula ##STR50##
2. A dyed or printed hydrophobic synthetic material produced by the process of claim 1.
3. The process of claim 1 wherein said hydrophobic synthetic material is a polyolefin, cellulose 21/2 acetate, cellulose triacetate or a polyester.
US05/597,018 1973-10-22 1975-07-18 Water-insoluble monoazo dyestuffs Expired - Lifetime US4002425A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US05/597,018 US4002425A (en) 1973-10-22 1975-07-18 Water-insoluble monoazo dyestuffs

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
DE19732352858 DE2352858A1 (en) 1973-10-22 1973-10-22 HYDRO-INSOLUBLE MONOAZO DYES AND PROCESS FOR THEIR MANUFACTURING
US05/516,360 US4006129A (en) 1973-10-22 1974-10-21 2-Nitro-4-aliphaticoxy-phenyl-azo-2,6-dihydroxy-3-cyano-4-methylpyridine compounds
DT2352858 1974-10-22
US05/597,018 US4002425A (en) 1973-10-22 1975-07-18 Water-insoluble monoazo dyestuffs

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US05/516,360 Division US4006129A (en) 1973-10-22 1974-10-21 2-Nitro-4-aliphaticoxy-phenyl-azo-2,6-dihydroxy-3-cyano-4-methylpyridine compounds

Publications (1)

Publication Number Publication Date
US4002425A true US4002425A (en) 1977-01-11

Family

ID=27185581

Family Applications (1)

Application Number Title Priority Date Filing Date
US05/597,018 Expired - Lifetime US4002425A (en) 1973-10-22 1975-07-18 Water-insoluble monoazo dyestuffs

Country Status (1)

Country Link
US (1) US4002425A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4134723A (en) * 1975-03-25 1979-01-16 Imperial Chemical Industries Limited Coloration process
US4559296A (en) * 1983-05-07 1985-12-17 Agfa-Gevaert Aktiengesellschaft Photographic recording material containing new azo dyes

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3487066A (en) * 1965-08-13 1969-12-30 Cassella Farbwerke Mainkur Ag Water-insoluble monoazo pyridine dyestuffs
US3869441A (en) * 1971-01-04 1975-03-04 Ici Ltd 3-secondary aminomethylene-4-lower-alkyl-5-azo-6-hydroxypyrid-2-one dyestuffs

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3487066A (en) * 1965-08-13 1969-12-30 Cassella Farbwerke Mainkur Ag Water-insoluble monoazo pyridine dyestuffs
US3869441A (en) * 1971-01-04 1975-03-04 Ici Ltd 3-secondary aminomethylene-4-lower-alkyl-5-azo-6-hydroxypyrid-2-one dyestuffs

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4134723A (en) * 1975-03-25 1979-01-16 Imperial Chemical Industries Limited Coloration process
US4559296A (en) * 1983-05-07 1985-12-17 Agfa-Gevaert Aktiengesellschaft Photographic recording material containing new azo dyes

Similar Documents

Publication Publication Date Title
US4550171A (en) 2-(Oxo, or thio)-3-substituted 1,3-benzothiazolyl-4-cyano-7-substituted amino-benzopyrans
US3905951A (en) Azo dyestuffs containing a 1-lower alkyl-6-hydroxypyrid-2-one coupling component
US5602238A (en) Azothiophene dyes containing a 2,4,6-triamino-3-cyanopyridine coupling component
US4006129A (en) 2-Nitro-4-aliphaticoxy-phenyl-azo-2,6-dihydroxy-3-cyano-4-methylpyridine compounds
US4002425A (en) Water-insoluble monoazo dyestuffs
US4062642A (en) Process for dyeing and printing synthetic fiber materials
US4111930A (en) Monoazo dyes having an aryloxyalkyl group on the nitrogen atom in the para position of a 1,4-phenylene coupling component radical
US4085099A (en) Water-insoluble nitrophenylazophenyl compounds containing a terminal --N--(C2)n --O--CO-- or --CO--O--CH2 --CH2 --C3 F5 group
CH498907A (en) Disperse monoazo dyes useful in dyeing linear aromatic
US3984199A (en) Water-insoluble monoazo dyestuffs
US4101543A (en) Benzene-azo-heterocyclic dyestuffs derived from alkyl aminocinnamates or aminocinnamide
US4087420A (en) Azo dyestuffs containing an α-phenylamino isobutyric acid alkyl ester coupling component
US4472307A (en) Preparation of anilino azo carbazole dyestuffs prepared by diazotization by nitrosylsulphuric acid in acetic acid
US4257943A (en) Disperse azo dyestuffs and process for preparation and their use
US3954396A (en) Dyeing synthetic materials with a dodecyl benzoicacid ester-azo-(3-cyano-4-methyl-6-hydroxy-2-pyridone)
US3993441A (en) 4-Nitro,2-alkylbenzene azo-3-cyano-4-methyl-6-hydroxy-2-pyridone dyeing of synthetic hydrophobic fibers
US4547579A (en) Substituted benzopyran compounds
DE1644260A1 (en) Process for the preparation of mono- and disazo dyes which are sparingly soluble in water
US4440681A (en) Water-insoluble monoazo dyestuffs and their preparation
US4035143A (en) Water-insoluble azo dyestuffs
US3071571A (en) Complex metal compounds of water-
US4529406A (en) Nitrothiazolyl-monoazo-2,2,4-trimethyl-1,2,3,4-tetrahydroquinoline compounds for polyester
US4008213A (en) Azo dyestuffs containing a cinnamonitrile residue
US4058518A (en) Water-insoluble monoazo 3-cyano-4-methyl-6-hydroxy-2-pyridine dyestuffs
US4704452A (en) Azo dyes containing aralkyl-nitrophenyl diazo components